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Session Recording 1 hr 27 min
MDR by the Numbers: Leveraging New Data for Implementation Planning
After the wake of the initial and then the first extension of the MDR deadline, the EU regulatory landscape is still reeling from the new requirements. Now facing the possibility of another extension, the medical device industry is further confused not only about requirements themselves but also if and when they must comply.
Specifically, this webinar will cover:
- Where MDR stands today - an extensive look at published data from competent authorities, notified bodies and industry stakeholders
- Review of recently published MCDG guidances
- Nuances of the MDR "Extension"
- What medical device professionals need to be doing
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